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Quality Engineer (Manufacturing, Science & Technology), Huddersfield
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Client:
Thornton & Ross
Location:
Huddersfield, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
d010ead30073
Job Views:
10
Posted:
26.04.2025
Expiry Date:
10.06.2025
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Job Description:
Quality Engineer
Manufacturing, Science & Technology
About the Company:
Thornton & Ross are one of the UK's fastest-growing, leading producers of household pharmaceutical products & own some of the country's most loved brands such as, as well as the leading disinfectant. Many people in the UK will have a product from Thornton & Ross somewhere at home. We are also a trusted & reliable provider of prescription products, including emollients, bone health products & generics to the NHS with 100 years’ heritage behind us.
We are part of the STADA group. STADA Arzneimittel AG is a German Stock Corporation with headquarters in Bad Vilbel, Germany. STADA focuses on a two-pillar strategy consisting of generics, including specialty pharmaceuticals & non-prescription consumer health products. Worldwide, STADA Arzneimittel AG sells its products in approximately 120 countries.
Like all success stories, our company history started with a great idea. In 1895, a group of pharmacists had a common objective: the standardised production of medicinal products to ensure an effective and reasonable provision of healthcare. This was the beginning of STADA’s impressive development. We are now a leading manufacturer of high-quality pharmaceuticals. With a long-standing heritage rooted in pharmacies, we continue to be a reliable and trustworthy partner. We help people regain and protect a dignified and able life. As STADA, we fundamentally care for people’s health as a trusted partner.
If you are ready for new challenges where you can make a difference to people’s health, you have come to the right place. We are looking for people with a great attitude and passion, who care about making a difference in the world.
About the Role:
The purpose of this role is to provide front line expert support for all process-specific issues to production within one or more production steps, to ensure execution of processes on-time, continuously improving in quality and efficiency, performed in compliance to cGMPs, SOPs and applicable guidelines and normatives. To implement the Technology Transfer/Commercialization of new products.
Main responsibilities include but are not limited to:
* Provide front line support to manufacturing, working with the shift teams, focusing on manufacturing each batch safely, on time, in compliance with the batch instructions and quality requirements.
* Support the completion of technology transfer project (as receiving site), commercialization and product launch of new products.
* Execute process validations, re-validations, Annual Monitoring Batch (AMB) and short-term improvement projects, liaising with all the relevant parties at shopfloor to ensure accurate execution.
* Review and assure that validation protocols and reports are technically correct.
* Ensure protocols are executed as intended.
* Write Manufacturing Process Transfer Documents (protocol, report).
* Provide expertise and identify and implement innovative validation best practices.
* Execute process improvements and scale-up.
About You:
At STADA we talk about diversity as Uniqueness. Everyone is unique and we recognise our differences as a strength. Our values Entrepreneurship, Integrity, Agility and One STADA ensure our uniqueness thrives, enabling us to care for people’s health as a trusted partner. Empower your Uniqueness, bring your whole self to STADA. If you’re keen to add value and see results, thrive in a busy fast paced environment and have the can-do spirit that’s spearheading our success, bring those qualities, with the following:
* Degree in Pharmacy, Pharmaceutical Technology, Chemistry or equivalent scientific degree or
* Combined experience in Pharmaceutical (i.e., Validation / QA) or allied industries with exposure to cGMP and GDP.
* Strong knowledge of pharmaceutical industry, specifically in production.
* Proficiency in English, both written and spoken
* In-depth knowledge of cGMPs and current validation sciences.
* Proven process understanding (Pharma, GMP, Regulatory aspects)
What’s in it for you?
Rewarding our employees is important to us, which is why we offer a range of fantastic benefits, such as:
* 25 days annual leave (plus bank holidays) and the opportunity to buy an additional 5 days leave.
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